CELLISYS EX EGF INTENSE MASK EGF- glycerin liquid

Cellisys EX EGF Intense Mask by

Drug Labeling and Warnings

Cellisys EX EGF Intense Mask by is a Otc medication manufactured, distributed, or labeled by DN Company Co., Ltd., C&TECH CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT: Glycerin 10%

INACTIVE INGREDIENT

INACTIVE INGREDIENTS: Water, Butylene Glycol, Caprylic/Capric Triglyceride, Alcohol, Hydrogenated Lecithin, 1,2-Hexanediol, Sodium Stearoyl Glutamate, Sodium Ascorbyl Phosphate, sh-Oligopeptide-1, TriethylHexanoin, etc.

PURPOSE

PURPOSE: Skin protectant

WARNINGS

WARNING: For external use only. Avoid contact with eyes. Discontinue use if signs of irritation or rash appear. Keep out of reach of babies and children.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of babies and children.

INDICATIONS AND USAGE

INDICATION AND USAGE:

1. Thoroughly cleanse face.
2. Unfold the mask and remove plastic sheet from mask.
3. Apply on face.
4. Wear the mask for 15 to 20minutes and peel off slowly from the edges. Massage remaining soloution into skin with hands.

DOSAGE AND ADMINISTRATION

DOSAGE AND ADMINISTRATION: Recommended interval for mask application is every 2~3 days for maximum efficiency. Wipe your body and neck with extra serum.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

CELLISYS EX EGF INTENSE MASK  EGF
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60565-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX)	GLYCERIN	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60565-011-01	20 g in 1 PACKAGE; Type 0: Not a Combination Product	03/01/2016

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part347	07/01/2013

Labeler - DN Company Co., Ltd. (688369859)

Registrant - DN Company Co., Ltd. (688369859)

Establishment
Name	Address	ID/FEI	Business Operations
C&TECH CORPORATION		688204698	manufacture(60565-011)